# Hydroxyzine Hydrochloride

NDC: 71656-090
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: Saptalis Pharmaceuticals, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260617

FDA application: ANDA220271

## Active ingredients

- HYDROXYZINE HYDROCHLORIDE: 10 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71656-090"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71656-090
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ab23881-334c-474d-9d93-25ea225548dc